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Volumn 72, Issue 7, 2007, Pages 2686-2689

Polyhydroxylated indolines and oxindoles from C-glycosides via sequential Henry reaction, Michael addition, and reductive amination/amidation

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; DERIVATIVES; KETONES; REDUCTION; SYNTHESIS (CHEMICAL);

EID: 34047241865     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo070014o     Document Type: Article
Times cited : (18)

References (59)
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    • (1990) Chem. Rev , vol.90 , pp. 1171-1202
    • Sinnott, M.L.1
  • 37
    • 34047205110 scopus 로고    scopus 로고
    • To avoid confusion in the assignment of NMR data, the carbon numbering used in this paper corresponds to the numbering of the original carbohydrates
    • To avoid confusion in the assignment of NMR data, the carbon numbering used in this paper corresponds to the numbering of the original carbohydrates.
  • 38
    • 0000851805 scopus 로고    scopus 로고
    • Trost, Fleming, Heathcock, Eds, Pergamon: Oxford
    • (a) Rosini, G. In Comprehensive Organic Synthesis; Trost, Fleming, Heathcock, Eds.; Pergamon: Oxford, 1996; Vol. 2, pp 321-340.
    • (1996) Comprehensive Organic Synthesis , vol.2 , pp. 321-340
    • Rosini, G.1
  • 41
    • 84917987245 scopus 로고
    • Synthesis of Monosaccharides
    • 2nd ed, Pigman, Horton, Eds, Academic Press: New York
    • (a) Hough, L.; Richardson, A. C. Synthesis of Monosaccharides. In The Carbohydrates: Chemistry and Biochemistry. 2nd ed.; Pigman, Horton, Eds.; Academic Press: New York, 1980: Vol. IA. pp 114-164.
    • (1980) The Carbohydrates: Chemistry and Biochemistry , vol.IA , pp. 114-164
    • Hough, L.1    Richardson, A.C.2
  • 42
    • 34047243176 scopus 로고    scopus 로고
    • Horton, D.; Wander, J. D. Amino Sugars. In The Carbohydrates: Chemistry and Biochemistry, 2nd ed.; Pigman, Horton, Eds.; Academic Press: New York, 1980; IB, pp 644-760.
    • (b) Horton, D.; Wander, J. D. Amino Sugars. In The Carbohydrates: Chemistry and Biochemistry, 2nd ed.; Pigman, Horton, Eds.; Academic Press: New York, 1980; Vol. IB, pp 644-760.
  • 48
    • 8444252168 scopus 로고    scopus 로고
    • For a recent review of catalytic asymmetric nitroaldol reactions, see
    • For a recent review of catalytic asymmetric nitroaldol reactions, see: Palomo, C.; Oiarbide, M.; Mielgo, A. Angew. Chem., Int. Ed. 2004. 43, 5442-5444.
    • (2004) Angew. Chem., Int. Ed , vol.43 , pp. 5442-5444
    • Palomo, C.1    Oiarbide, M.2    Mielgo, A.3
  • 55
    • 34047202722 scopus 로고    scopus 로고
    • We also treated substrate 6 under the same conditions, but the reaction was extremely slow.
    • We also treated substrate 6 under the same conditions, but the reaction was extremely slow.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.